Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8437 |
| ensemblid | ENSG00000111344.12 |
| hgncid | 9873 |
| symbol | RASAL1 |
| name | RAS protein activator like 1 |
| refseq_nuc | NM_001301202.2 |
| refseq_prot | NP_001288131.1 |
| ensembl_nuc | ENST00000548055.2 |
| ensembl_prot | ENSP00000448510.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 113099278 |
| end | 113135761 |
| strand | - |
| ver | v1.2 |
| region | chr12:113099278-113135761 |
| region5000 | chr12:113094278-113140761 |
| regionname0 | RASAL1_chr12_113099278_113135761 |
| regionname5000 | RASAL1_chr12_113094278_113140761 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 805 | 222 | 53 | 47 | 83 | 10 | 28 | 60 | RASAL1_chr12_113094278_113140761 | RASAL1 | MAKSS others(800): Show |
chr12 | 113094278 | 113140761 |
| a0002 | 1/0 | 805 | 83 | 25 | 6 | 41 | 3 | 7 | 35 | RASAL1_chr12_113094278_113140761 | RASAL1 | MAKSS others(800): Show |
chr12 | 113094278 | 113140761 |
| a0003 | 0/0 | 805 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | MAKSS others(800): Show |
chr12 | 113094278 | 113140761 |
| a0004 | 0/0 | 805 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | MAKSS others(800): Show |
chr12 | 113094278 | 113140761 |
| a0005 | 0/0 | 691 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | MAKSS others(686): Show |
chr12 | 113094278 | 113140761 |
| a0006 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | MAKSS others(800): Show |
chr12 | 113094278 | 113140761 |
| a0007 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | MAKSS others(800): Show |
chr12 | 113094278 | 113140761 |
| a0008 | 0/0 | 805 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | MAKSS others(800): Show |
chr12 | 113094278 | 113140761 |
| a0009 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | MAKSS others(800): Show |
chr12 | 113094278 | 113140761 |
| a0010 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | MAKSS others(800): Show |
chr12 | 113094278 | 113140761 |
| a0011 | 0/0 | 805 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | MAKSS others(800): Show |
chr12 | 113094278 | 113140761 |
| a0012 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | MAKSS others(800): Show |
chr12 | 113094278 | 113140761 |
| a0013 | 0/0 | 805 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | MAKSS others(800): Show |
chr12 | 113094278 | 113140761 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2415 | 208 | 46 | 45 | 80 | 10 | 26 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0001c0004 | 0/0 | 2415 | 4 | 3 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0001c0005 | 0/0 | 2415 | 3 | 2 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0001c0007 | 0/0 | 2415 | 3 | 0 | 0 | 2 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0001c0011 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0001c0013 | 0/0 | 2415 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0001c0017 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0001c0022 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0002c0002 | 1/0 | 2415 | 53 | 21 | 5 | 19 | 1 | 6 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0002c0003 | 0/0 | 2415 | 22 | 0 | 0 | 22 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0002c0006 | 0/0 | 2415 | 3 | 0 | 1 | 0 | 2 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0002c0008 | 0/0 | 2415 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0002c0018 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0002c0019 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0002c0025 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0003c0010 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0004c0012 | 0/0 | 2415 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0005c0014 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0006c0009 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0007c0021 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0008c0023 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0009c0015 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0010c0016 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0011c0020 | 0/0 | 2415 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0012c0026 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 | ||
| a0013c0024 | 0/0 | 2415 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | ATGGC others(2410): Show |
chr12 | 113094278 | 113140761 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3368 | 202 | 44 | 45 | 78 | 10 | 24 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0001c0001t0002 | 0/0 | 3368 | 2 | 0 | 0 | 1 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0001c0001t0003 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0001c0001t0008 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0001c0001t0009 | 0/0 | 3368 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0001c0001t0010 | 0/0 | 3368 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0001c0004t0001 | 0/0 | 3368 | 4 | 3 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0001c0005t0001 | 0/0 | 3368 | 3 | 2 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0001c0007t0001 | 0/0 | 3368 | 3 | 0 | 0 | 2 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0001c0011t0001 | 0/0 | 3368 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0001c0013t0001 | 0/0 | 3368 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0001c0017t0001 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0001c0022t0001 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0002c0002t0001 | 0/0 | 3368 | 13 | 10 | 2 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0002c0002t0002 | 1/0 | 3368 | 36 | 7 | 3 | 19 | 1 | 5 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0002c0002t0003 | 0/0 | 3368 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0002c0002t0006 | 0/0 | 3368 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0002c0003t0001 | 0/0 | 3368 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0002c0003t0002 | 0/0 | 3368 | 21 | 0 | 0 | 21 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0002c0006t0004 | 0/0 | 3368 | 3 | 0 | 1 | 0 | 2 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0002c0008t0005 | 0/0 | 3368 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0002c0018t0004 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0002c0019t0003 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0002c0025t0004 | 0/0 | 3368 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0003c0010t0007 | 0/0 | 3368 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0004c0012t0001 | 0/0 | 3368 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0005c0014t0001 | 0/0 | 3368 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0006c0009t0002 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0007c0021t0001 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0008c0023t0005 | 0/0 | 3368 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0009c0015t0001 | 0/0 | 3368 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0010c0016t0001 | 0/0 | 3368 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0011c0020t0002 | 0/0 | 3368 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0012c0026t0002 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| a0013c0024t0003 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | GCCCA others(3363): Show |
chr12 | 113094278 | 113140761 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 0 | 3 | 7 | 0 | 3 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 3 | 5 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0007 | 0/0 | 5 | 1 | 1 | 0 | 1 | 2 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0009 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0009g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0001t0010g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0004t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0005t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0005t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0007t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0007t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0007t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0011t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0013t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0017t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0001c0022t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0004 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0002t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0006t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0006t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0006t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0008t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0008t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0018t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0019t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0002c0025t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0003c0010t0007g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0004c0012t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0005c0014t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0006c0009t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0007c0021t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0008c0023t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0009c0015t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0010c0016t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0011c0020t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0012c0026t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| a0013c0024t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0006 | t0004 | g0195 | EUR | GBR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | GBR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00280 | hp1 | a0002 | c0006 | t0004 | g0201 | EUR | FIN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00280 | hp2 | a0003 | c0010 | t0007 | g0029 | EUR | FIN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00438 | hp2 | a0002 | c0003 | t0002 | g0075 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0118 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0231 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01109 | hp1 | a0001 | c0005 | t0001 | g0155 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01346 | hp1 | a0004 | c0012 | t0001 | g0126 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01358 | hp2 | a0002 | c0006 | t0004 | g0089 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01993 | hp2 | a0001 | c0013 | t0001 | g0223 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02055 | hp1 | a0002 | c0002 | t0006 | g0034 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0149 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02071 | hp2 | a0002 | c0003 | t0002 | g0069 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02132 | hp2 | a0005 | c0014 | t0001 | g0091 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0218 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02155 | hp1 | a0002 | c0003 | t0002 | g0081 | EAS | CDX | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CDX | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CDX | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0190 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0232 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0028 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02572 | hp2 | a0002 | c0008 | t0005 | g0039 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02615 | hp2 | a0002 | c0002 | t0003 | g0037 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02622 | hp1 | a0001 | c0017 | t0001 | g0226 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02622 | hp2 | a0006 | c0009 | t0002 | g0038 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0054 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02698 | hp2 | a0001 | c0001 | t0010 | g0236 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0176 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02738 | hp2 | a0001 | c0011 | t0001 | g0202 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0046 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0035 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0028 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0027 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02976 | hp1 | a0007 | c0021 | t0001 | g0215 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0161 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0233 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0027 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03139 | hp1 | a0001 | c0022 | t0001 | g0094 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0064 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03209 | hp1 | a0002 | c0018 | t0004 | g0041 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03209 | hp2 | a0001 | c0005 | t0001 | g0221 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0047 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0015 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03486 | hp2 | a0002 | c0019 | t0003 | g0033 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0120 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0234 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0052 | SAS | PJL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0119 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG04115 | hp1 | a0001 | c0007 | t0001 | g0082 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG04184 | hp2 | a0002 | c0025 | t0004 | g0103 | SAS | BEB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG04228 | hp2 | a0008 | c0023 | t0005 | g0111 | SAS | STU | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18522 | hp1 | a0001 | c0005 | t0001 | g0157 | AFR | YRI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18945 | hp2 | a0001 | c0007 | t0001 | g0072 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18946 | hp2 | a0002 | c0003 | t0002 | g0077 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18949 | hp1 | a0009 | c0015 | t0001 | g0151 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18950 | hp1 | a0010 | c0016 | t0001 | g0097 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18950 | hp2 | a0001 | c0001 | t0009 | g0209 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18951 | hp1 | a0002 | c0003 | t0002 | g0071 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18954 | hp1 | a0002 | c0003 | t0002 | g0080 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18956 | hp1 | a0002 | c0003 | t0002 | g0228 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18957 | hp1 | a0002 | c0003 | t0002 | g0079 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18961 | hp1 | a0002 | c0003 | t0002 | g0073 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18962 | hp1 | a0002 | c0003 | t0001 | g0074 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18969 | hp1 | a0002 | c0003 | t0002 | g0008 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18969 | hp2 | a0011 | c0020 | t0002 | g0055 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18974 | hp2 | a0002 | c0003 | t0002 | g0084 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18977 | hp2 | a0002 | c0003 | t0002 | g0076 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18979 | hp2 | a0002 | c0003 | t0002 | g0068 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18984 | hp1 | a0001 | c0004 | t0001 | g0189 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18984 | hp2 | a0002 | c0003 | t0002 | g0066 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18992 | hp2 | a0002 | c0003 | t0002 | g0008 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19043 | hp1 | a0012 | c0026 | t0002 | g0048 | AFR | LWK | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19043 | hp2 | a0002 | c0002 | t0006 | g0032 | AFR | LWK | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19063 | hp1 | a0002 | c0003 | t0002 | g0083 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19064 | hp1 | a0002 | c0003 | t0002 | g0110 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19065 | hp1 | a0001 | c0007 | t0001 | g0070 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19066 | hp1 | a0002 | c0003 | t0002 | g0008 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19070 | hp1 | a0002 | c0003 | t0002 | g0078 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19074 | hp1 | a0002 | c0003 | t0002 | g0008 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19075 | hp1 | a0002 | c0003 | t0002 | g0067 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | YRI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ASW | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA20129 | hp2 | a0013 | c0024 | t0003 | g0036 | AFR | ASW | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0178 | EUR | TSI | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0137 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG02559 | hp2 | a0002 | c0002 | t0003 | g0030 | AFR | ACB | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03471 | hp1 | a0002 | c0008 | t0005 | g0040 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0205 | REF | REF | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0177 | REF | REF | RASAL1_chr12_113094278_113140761 | RASAL1 | chr12 | 113094278 | 113140761 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113103975 | C | T | 1 | a0005 | 1 | HG02132.hp2 | stop_gained | HIGH | c.2075G>A | p.Trp692* | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/21 | 2374/3368 | 2075/2418 | 692/805 | chr12 | 113103975 | |||
| chr12:113105737 | A | G | 1 | a0004 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.1807T>C | p.Phe603Leu | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/21 | 2106/3368 | 1807/2418 | 603/805 | chr12 | 113105737 | |||
| chr12:113105800 | C | G | 1 | a0009 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.1744G>C | p.Gly582Arg | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/21 | 2043/3368 | 1744/2418 | 582/805 | chr12 | 113105800 | |||
| chr12:113105802 | G | C | 1 | a0009 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.1742C>G | p.Ala581Gly | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/21 | 2041/3368 | 1742/2418 | 581/805 | chr12 | 113105802 | |||
| chr12:113105803 | C | A | 1 | a0009 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.1741G>T | p.Ala581Ser | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/21 | 2040/3368 | 1741/2418 | 581/805 | chr12 | 113105803 | |||
| chr12:113107125 | G | C | 1 | a0011 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.1629C>G | p.Asp543Glu | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/21 | 1928/3368 | 1629/2418 | 543/805 | chr12 | 113107125 | |||
| chr12:113112093 | T | G | 1 | a0010 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.1367A>C | p.Glu456Ala | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/21 | 1666/3368 | 1367/2418 | 456/805 | chr12 | 113112093 | |||
| chr12:113115676 | C | T | 7 | a0001 a0004 a0005 others(4): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
missense_variant | MODERATE | c.962G>A | p.Arg321His | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 10/21 | 1261/3368 | 962/2418 | 321/805 | chr12 | 113115676 | |||
| chr12:113116005 | G | A | 2 | a0007 a0012 |
2 | HG02976.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.778C>T | p.Arg260Cys | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 9/21 | 1077/3368 | 778/2418 | 260/805 | chr12 | 113116005 | |||
| chr12:113127832 | G | A | 1 | a0008 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.278C>T | p.Ala93Val | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/21 | 577/3368 | 278/2418 | 93/805 | chr12 | 113127832 | |||
| chr12:113127847 | G | A | 1 | a0013 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.263C>T | p.Ser88Leu | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/21 | 562/3368 | 263/2418 | 88/805 | chr12 | 113127847 | |||
| chr12:113128128 | G | A | 1 | a0003 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.173C>T | p.Thr58Met | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/21 | 472/3368 | 173/2418 | 58/805 | chr12 | 113128128 | |||
| chr12:113135432 | C | G | 2 | a0003 a0006 |
2 | HG00280.hp2 HG02622.hp2 |
missense_variant | MODERATE | c.31G>C | p.Val11Leu | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/21 | 330/3368 | 31/2418 | 11/805 | chr12 | 113135432 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113099959 | C | T | 1 | a0002c0018 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.2388G>A | p.Gly796Gly | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 21/21 | 2687/3368 | 2388/2418 | 796/805 | chr12 | 113099959 | |||
| chr12:113099968 | C | T | 4 | a0002c0006 a0002c0018 a0002c0025 others(1): Show |
6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
synonymous_variant | LOW | c.2379G>A | p.Gln793Gln | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 21/21 | 2678/3368 | 2379/2418 | 793/805 | chr12 | 113099968 | |||
| chr12:113102008 | G | A | 1 | a0001c0005 | 3 | HG01109.hp1 HG03209.hp2 NA18522.hp1 |
splice_region_variant&synonymous_variant | LOW | c.2106C>T | p.Ala702Ala | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/21 | 2405/3368 | 2106/2418 | 702/805 | chr12 | 113102008 | |||
| chr12:113103995 | A | T | 1 | a0009c0015 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.2055T>A | p.Gly685Gly | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/21 | 2354/3368 | 2055/2418 | 685/805 | chr12 | 113103995 | |||
| chr12:113104194 | C | T | 1 | a0001c0013 | 1 | HG01993.hp2 | synonymous_variant | LOW | c.1935G>A | p.Thr645Thr | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 17/21 | 2234/3368 | 1935/2418 | 645/805 | chr12 | 113104194 | |||
| chr12:113104293 | A | G | 5 | a0002c0006 a0002c0008 a0002c0018 others(2): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
synonymous_variant | LOW | c.1836T>C | p.Cys612Cys | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 17/21 | 2135/3368 | 1836/2418 | 612/805 | chr12 | 113104293 | |||
| chr12:113105753 | G | A | 1 | a0002c0019 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1791C>T | p.Ser597Ser | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/21 | 2090/3368 | 1791/2418 | 597/805 | chr12 | 113105753 | |||
| chr12:113114889 | G | A | 1 | a0001c0017 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1092C>T | p.His364His | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/21 | 1391/3368 | 1092/2418 | 364/805 | chr12 | 113114889 | |||
| chr12:113117141 | G | A | 3 | a0002c0006 a0002c0025 a0003c0010 |
5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
synonymous_variant | LOW | c.663C>T | p.Thr221Thr | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/21 | 962/3368 | 663/2418 | 221/805 | chr12 | 113117141 | |||
| chr12:113127822 | G | A | 1 | a0001c0022 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.288C>T | p.Ala96Ala | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/21 | 587/3368 | 288/2418 | 96/805 | chr12 | 113127822 | |||
| chr12:113127858 | G | A | 1 | a0002c0025 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.252C>T | p.Ile84Ile | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/21 | 551/3368 | 252/2418 | 84/805 | chr12 | 113127858 | |||
| chr12:113127870 | G | A | 2 | a0001c0004 a0012c0026 |
5 | HG02717.hp2 HG03195.hp1 HG03486.hp1 others(2): Show |
synonymous_variant | LOW | c.240C>T | p.His80His | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/21 | 539/3368 | 240/2418 | 80/805 | chr12 | 113127870 | |||
| chr12:113128084 | G | A | 2 | a0001c0007 a0002c0003 |
25 | HG00438.hp2 HG02071.hp2 HG02155.hp1 others(22): Show |
synonymous_variant | LOW | c.217C>T | p.Leu73Leu | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/21 | 516/3368 | 217/2418 | 73/805 | chr12 | 113128084 | |||
| chr12:113128127 | C | T | 1 | a0001c0011 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.174G>A | p.Thr58Thr | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/21 | 473/3368 | 174/2418 | 58/805 | chr12 | 113128127 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113099321 | G | A | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(25): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*608C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 21/21 | 608 | chr12 | 113099321 | ||||||
| chr12:113099416 | C | T | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0009 others(22): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*513G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 21/21 | 513 | chr12 | 113099416 | ||||||
| chr12:113099418 | C | G | 1 | a0001c0001t0009 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*511G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 21/21 | 511 | chr12 | 113099418 | ||||||
| chr12:113099553 | C | T | 4 | a0002c0006t0004 a0002c0018t0004 a0002c0025t0004 others(1): Show |
6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*376G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 21/21 | 376 | chr12 | 113099553 | ||||||
| chr12:113099757 | C | T | 4 | a0002c0006t0004 a0002c0018t0004 a0002c0025t0004 others(1): Show |
6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*172G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 21/21 | 172 | chr12 | 113099757 | ||||||
| chr12:113135652 | C | G | 1 | a0003c0010t0007 | 1 | HG00280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-190G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/21 | 190 | chr12 | 113135652 | ||||||
| chr12:113135682 | T | G | 1 | a0001c0001t0010 | 1 | HG02698.hp2 | 5_prime_UTR_variant | MODIFIER | c.-220A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/21 | 220 | chr12 | 113135682 | ||||||
| chr12:113135695 | A | C | 7 | a0001c0001t0003 a0001c0001t0008 a0002c0002t0003 others(4): Show |
9 | HG00280.hp2 HG02055.hp1 HG02559.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-233T>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/21 | 233 | chr12 | 113135695 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113100147 | T | C | 2 | a0002c0002t0001g0047 a0002c0019t0003g0033 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2279-79A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100147 | |||||||
| chr12:113100228 | T | C | 6 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(3): Show |
6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2279-160A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100228 | |||||||
| chr12:113100262 | T | C | 1 | a0002c0002t0001g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2279-194A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100262 | |||||||
| chr12:113100309 | T | G | 4 | a0001c0001t0008g0035 a0002c0008t0005g0039 a0002c0008t0005g0040 others(1): Show |
4 | HG02572.hp2 HG02809.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2279-241A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100309 | |||||||
| chr12:113100359 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2278+269G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100359 | |||||||
| chr12:113100407 | T | C | 5 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(2): Show |
5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2278+221A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100407 | |||||||
| chr12:113100407 | T | G | 1 | a0002c0018t0004g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2278+221A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100407 | |||||||
| chr12:113100610 | A | T | 6 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(3): Show |
6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2278+18T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 20/20 | chr12 | 113100610 | |||||||
| chr12:113100793 | C | CCAT | 3 | a0001c0001t0001g0166 a0001c0001t0001g0168 a0001c0001t0001g0183 |
3 | NA18992.hp1 NA19009.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.2226-116_2226-114d others(5): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113100793 | |||||||
| chr12:113101011 | T | C | 2 | a0002c0002t0001g0047 a0002c0019t0003g0033 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2226-331A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101011 | |||||||
| chr12:113101182 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2226-502C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101182 | |||||||
| chr12:113101196 | A | T | 2 | a0002c0002t0001g0047 a0002c0019t0003g0033 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2226-516T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101196 | |||||||
| chr12:113101267 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2226-587G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101267 | |||||||
| chr12:113101433 | A | T | 2 | a0001c0001t0001g0134 a0008c0023t0005g0111 |
2 | HG04228.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2225+456T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101433 | |||||||
| chr12:113101571 | C | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.2225+318G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101571 | |||||||
| chr12:113101656 | GCTCCAGG others(40): Show |
G | 6 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(3): Show |
6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2225+186_2225+232d others(49): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101656 | |||||||
| chr12:113101759 | T | C | 18 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0122 others(15): Show |
24 | HG01081.hp2 HG01109.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.2225+130A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 19/20 | chr12 | 113101759 | |||||||
| chr12:113102017 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
splice_region_variant&intron_variant | LOW | c.2105-8T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102017 | |||||||
| chr12:113102024 | C | T | 6 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(3): Show |
6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2105-15G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102024 | |||||||
| chr12:113102067 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2105-58G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102067 | |||||||
| chr12:113102079 | C | A | 1 | a0002c0002t0001g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2105-70G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102079 | |||||||
| chr12:113102144 | G | A | 1 | a0002c0002t0001g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2105-135C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102144 | |||||||
| chr12:113102170 | C | G | 5 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(2): Show |
7 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2105-161G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102170 | |||||||
| chr12:113102207 | A | G | 1 | a0002c0025t0004g0103 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2105-198T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102207 | |||||||
| chr12:113102296 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2105-287C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102296 | |||||||
| chr12:113102468 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2105-459C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102468 | |||||||
| chr12:113102567 | C | A | 10 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(7): Show |
10 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2105-558G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102567 | |||||||
| chr12:113102580 | C | T | 1 | a0002c0002t0001g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2105-571G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102580 | |||||||
| chr12:113102595 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2105-586C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102595 | |||||||
| chr12:113102681 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2105-672G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102681 | |||||||
| chr12:113102711 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2105-702G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102711 | |||||||
| chr12:113102725 | A | G | 1 | a0002c0002t0006g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2105-716T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102725 | |||||||
| chr12:113102750 | T | G | 1 | a0001c0001t0001g0020 | 2 | HG01099.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.2105-741A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102750 | |||||||
| chr12:113102828 | A | G | 6 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(3): Show |
8 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2105-819T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102828 | |||||||
| chr12:113102829 | C | T | 6 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(3): Show |
8 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2105-820G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102829 | |||||||
| chr12:113102912 | A | G | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2105-903T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102912 | |||||||
| chr12:113102958 | C | T | 2 | a0002c0008t0005g0039 a0002c0008t0005g0040 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2105-949G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113102958 | |||||||
| chr12:113103174 | TTTATATA others(3): Show |
T | 1 | a0002c0019t0003g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2104+762_2104+771d others(12): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103174 | |||||||
| chr12:113103178 | T | C | 1 | a0002c0018t0004g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2104+768A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103178 | |||||||
| chr12:113103179 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2104+767T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103179 | |||||||
| chr12:113103187 | T | A | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2104+759A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103187 | |||||||
| chr12:113103234 | GTTA | G | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2104+709_2104+711d others(5): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103234 | |||||||
| chr12:113103282 | T | C | 1 | a0002c0002t0001g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2104+664A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103282 | |||||||
| chr12:113103343 | G | C | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2104+603C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103343 | |||||||
| chr12:113103419 | A | G | 1 | a0002c0002t0001g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2104+527T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103419 | |||||||
| chr12:113103426 | G | T | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2104+520C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103426 | |||||||
| chr12:113103605 | C | CA | 27 | a0001c0001t0001g0090 a0001c0001t0001g0165 a0001c0001t0001g0170 others(24): Show |
35 | HG00642.hp1 HG01123.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.2104+340dupT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103605 | |||||||
| chr12:113103659 | A | G | 6 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0148 others(3): Show |
8 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2104+287T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103659 | |||||||
| chr12:113103669 | A | G | 5 | a0002c0002t0002g0043 a0002c0002t0002g0044 a0002c0002t0002g0045 others(2): Show |
5 | HG02148.hp1 NA18960.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.2104+277T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103669 | |||||||
| chr12:113103891 | C | A | 1 | a0009c0015t0001g0151 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2104+55G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 18/20 | chr12 | 113103891 | |||||||
| chr12:113104099 | C | A | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1969-18G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 17/20 | chr12 | 113104099 | |||||||
| chr12:113104135 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.1968+26G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 17/20 | chr12 | 113104135 | |||||||
| chr12:113104626 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1831-328G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104626 | |||||||
| chr12:113104646 | C | T | 2 | a0002c0002t0001g0047 a0002c0019t0003g0033 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1831-348G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104646 | |||||||
| chr12:113104657 | G | A | 1 | a0002c0002t0001g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1831-359C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104657 | |||||||
| chr12:113104712 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1831-414C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104712 | |||||||
| chr12:113104740 | G | A | 1 | a0002c0002t0006g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1831-442C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104740 | |||||||
| chr12:113104743 | C | G | 1 | a0008c0023t0005g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1831-445G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104743 | |||||||
| chr12:113104752 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1831-454G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104752 | |||||||
| chr12:113104754 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1831-456C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104754 | |||||||
| chr12:113104803 | C | T | 5 | a0002c0002t0002g0043 a0002c0002t0002g0044 a0002c0002t0002g0045 others(2): Show |
5 | HG02148.hp1 NA18960.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1831-505G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104803 | |||||||
| chr12:113104904 | A | G | 2 | a0002c0008t0005g0039 a0002c0008t0005g0040 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1831-606T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113104904 | |||||||
| chr12:113105056 | A | G | 1 | a0002c0019t0003g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1830+658T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105056 | |||||||
| chr12:113105155 | G | A | 6 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(3): Show |
6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1830+559C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105155 | |||||||
| chr12:113105202 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1830+512G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105202 | |||||||
| chr12:113105308 | C | T | 1 | a0001c0001t0008g0035 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1830+406G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105308 | |||||||
| chr12:113105309 | G | A | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1830+405C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105309 | |||||||
| chr12:113105418 | T | C | 3 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0231 |
3 | HG00642.hp1 HG00733.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1830+296A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105418 | |||||||
| chr12:113105426 | A | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1830+288T>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105426 | |||||||
| chr12:113105472 | G | A | 5 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(2): Show |
7 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1830+242C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105472 | |||||||
| chr12:113105508 | G | A | 1 | a0002c0002t0002g0054 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1830+206C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105508 | |||||||
| chr12:113105697 | G | A | 1 | a0002c0002t0001g0046 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1830+17C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 16/20 | chr12 | 113105697 | |||||||
| chr12:113105936 | G | T | 1 | a0013c0024t0003g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1658-50C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113105936 | |||||||
| chr12:113106023 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
209 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.1658-137C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106023 | |||||||
| chr12:113106077 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1658-191C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106077 | |||||||
| chr12:113106127 | G | T | 9 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0118 others(6): Show |
11 | HG00642.hp1 HG00733.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1658-241C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106127 | |||||||
| chr12:113106146 | C | G | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1658-260G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106146 | |||||||
| chr12:113106147 | C | A | 1 | a0013c0024t0003g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1658-261G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106147 | |||||||
| chr12:113106219 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1658-333C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106219 | |||||||
| chr12:113106262 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1658-376G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106262 | |||||||
| chr12:113106371 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1658-485G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106371 | |||||||
| chr12:113106384 | A | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1658-498T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106384 | |||||||
| chr12:113106564 | C | T | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1657+533G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106564 | |||||||
| chr12:113106572 | G | A | 9 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0118 others(6): Show |
11 | HG00642.hp1 HG00733.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1657+525C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106572 | |||||||
| chr12:113106650 | C | CT | 12 | a0001c0001t0001g0092 a0001c0001t0001g0191 a0001c0001t0008g0035 others(9): Show |
12 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1657+446dupA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106650 | |||||||
| chr12:113106747 | G | C | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1657+350C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106747 | |||||||
| chr12:113106765 | TTC | T | 5 | a0002c0002t0002g0043 a0002c0002t0002g0044 a0002c0002t0002g0045 others(2): Show |
5 | HG02148.hp1 NA18960.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1657+330_1657+331d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106765 | |||||||
| chr12:113106827 | G | A | 1 | a0013c0024t0003g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1657+270C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113106827 | |||||||
| chr12:113107038 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0169 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1657+59G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113107038 | |||||||
| chr12:113107069 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1657+28G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 15/20 | chr12 | 113107069 | |||||||
| chr12:113107266 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1513-25G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107266 | |||||||
| chr12:113107267 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1513-26C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107267 | |||||||
| chr12:113107360 | T | C | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1513-119A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107360 | |||||||
| chr12:113107388 | C | T | 2 | a0002c0003t0002g0079 a0002c0003t0002g0080 |
2 | NA18954.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1513-147G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107388 | |||||||
| chr12:113107426 | G | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1513-185C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107426 | |||||||
| chr12:113107442 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1513-201C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107442 | |||||||
| chr12:113107588 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.1513-347T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107588 | |||||||
| chr12:113107687 | T | C | 1 | a0002c0018t0004g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1512+398A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107687 | |||||||
| chr12:113107771 | A | C | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1512+314T>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107771 | |||||||
| chr12:113107773 | G | GC | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1512+311_1512+312i others(3): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107773 | |||||||
| chr12:113107774 | G | A | 1 | a0002c0018t0004g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1512+311C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107774 | |||||||
| chr12:113107805 | C | T | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1512+280G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107805 | |||||||
| chr12:113107892 | T | C | 1 | a0002c0002t0002g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1512+193A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107892 | |||||||
| chr12:113107953 | G | A | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1512+132C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107953 | |||||||
| chr12:113107982 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1512+103T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 14/20 | chr12 | 113107982 | |||||||
| chr12:113108355 | G | T | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-133C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108355 | |||||||
| chr12:113108427 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1375-205A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108427 | |||||||
| chr12:113108451 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1375-229A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108451 | |||||||
| chr12:113108620 | C | T | 1 | a0002c0002t0006g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1375-398G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108620 | |||||||
| chr12:113108672 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1375-450C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108672 | |||||||
| chr12:113108740 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1375-518T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108740 | |||||||
| chr12:113108828 | T | C | 2 | a0001c0001t0008g0035 a0002c0002t0001g0047 |
2 | HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1375-606A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108828 | |||||||
| chr12:113108837 | C | CT | 6 | a0002c0002t0002g0176 a0002c0006t0004g0089 a0002c0006t0004g0195 others(3): Show |
6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1375-616dupA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108837 | |||||||
| chr12:113108837 | CT | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1375-616delA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108837 | |||||||
| chr12:113108837 | CTT | C | 11 | a0001c0001t0001g0017 a0001c0001t0001g0116 a0001c0001t0001g0117 others(8): Show |
12 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1375-617_1375-616d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108837 | |||||||
| chr12:113108875 | T | C | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-653A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113108875 | |||||||
| chr12:113109035 | TTGTGTG | T | 6 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(3): Show |
6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1375-819_1375-814d others(8): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109035 | |||||||
| chr12:113109037 | G | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1375-815C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109037 | |||||||
| chr12:113109039 | G | T | 2 | a0001c0001t0001g0019 a0001c0001t0008g0035 |
3 | HG02602.hp2 HG02809.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1375-817C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109039 | |||||||
| chr12:113109043 | G | T | 6 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(3): Show |
6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1375-821C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109043 | |||||||
| chr12:113109043 | GT | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(88): Show |
128 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.1375-822delA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109043 | |||||||
| chr12:113109043 | GTT | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(102): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.1375-823_1375-822d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109043 | |||||||
| chr12:113109045 | T | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0105 a0002c0003t0002g0008 |
4 | HG01515.hp2 HG02602.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1375-823A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109045 | |||||||
| chr12:113109046 | T | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0093 a0001c0001t0001g0217 others(6): Show |
10 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1375-824A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109046 | |||||||
| chr12:113109047 | T | G | 1 | a0002c0018t0004g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1375-825A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109047 | |||||||
| chr12:113109048 | T | G | 1 | a0002c0002t0001g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1375-826A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109048 | |||||||
| chr12:113109059 | T | A | 5 | a0002c0002t0002g0043 a0002c0002t0002g0044 a0002c0002t0002g0045 others(2): Show |
5 | HG02148.hp1 NA18960.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1375-837A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109059 | |||||||
| chr12:113109124 | A | G | 1 | a0002c0008t0005g0039 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1375-902T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109124 | |||||||
| chr12:113109128 | G | A | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-906C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109128 | |||||||
| chr12:113109133 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1375-911T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109133 | |||||||
| chr12:113109211 | C | T | 5 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(2): Show |
5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1375-989G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109211 | |||||||
| chr12:113109215 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1375-993G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109215 | |||||||
| chr12:113109618 | G | C | 2 | a0002c0008t0005g0039 a0002c0008t0005g0040 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1375-1396C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109618 | |||||||
| chr12:113109681 | G | A | 1 | a0002c0018t0004g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1375-1459C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109681 | |||||||
| chr12:113109756 | G | T | 1 | a0010c0016t0001g0097 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1375-1534C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109756 | |||||||
| chr12:113109904 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1375-1682T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109904 | |||||||
| chr12:113109909 | C | A | 1 | a0008c0023t0005g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1375-1687G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109909 | |||||||
| chr12:113109951 | G | A | 1 | a0007c0021t0001g0215 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1375-1729C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109951 | |||||||
| chr12:113109960 | G | A | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-1738C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109960 | |||||||
| chr12:113109977 | G | C | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-1755C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113109977 | |||||||
| chr12:113110005 | C | A | 4 | a0001c0001t0008g0035 a0002c0002t0001g0047 a0002c0002t0006g0034 others(1): Show |
4 | HG02055.hp1 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1375-1783G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110005 | |||||||
| chr12:113110354 | G | A | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1374+1732C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110354 | |||||||
| chr12:113110438 | T | C | 35 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(32): Show |
57 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1374+1648A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110438 | |||||||
| chr12:113110448 | T | C | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1374+1638A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110448 | |||||||
| chr12:113110499 | G | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0093 |
3 | HG02015.hp1 HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1374+1587C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110499 | |||||||
| chr12:113110570 | A | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.1374+1516T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110570 | |||||||
| chr12:113110582 | T | C | 35 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(32): Show |
57 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1374+1504A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110582 | |||||||
| chr12:113110614 | T | A | 1 | a0001c0001t0008g0035 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1374+1472A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110614 | |||||||
| chr12:113110668 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1374+1418G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113110668 | |||||||
| chr12:113111071 | A | G | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1374+1015T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111071 | |||||||
| chr12:113111074 | T | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1374+1012A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111074 | |||||||
| chr12:113111094 | CTG | C | 12 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0098 others(9): Show |
15 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1374+990_1374+991d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111094 | |||||||
| chr12:113111098 | T | C | 13 | a0001c0001t0008g0035 a0002c0002t0001g0047 a0002c0002t0006g0034 others(10): Show |
13 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1374+988A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111098 | |||||||
| chr12:113111118 | G | A | 1 | a0013c0024t0003g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1374+968C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111118 | |||||||
| chr12:113111217 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0115 |
2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1374+869C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111217 | |||||||
| chr12:113111322 | G | C | 1 | a0002c0002t0001g0118 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1374+764C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111322 | |||||||
| chr12:113111610 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1374+476A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111610 | |||||||
| chr12:113111913 | A | T | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1374+173T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113111913 | |||||||
| chr12:113112028 | G | T | 1 | a0012c0026t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1374+58C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 13/20 | chr12 | 113112028 | |||||||
| chr12:113112382 | C | A | 1 | a0002c0002t0002g0178 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1182-104G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112382 | |||||||
| chr12:113112530 | C | T | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-252G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112530 | |||||||
| chr12:113112541 | C | G | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-263G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112541 | |||||||
| chr12:113112649 | C | G | 1 | a0012c0026t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1182-371G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112649 | |||||||
| chr12:113112766 | C | T | 1 | a0002c0002t0002g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1182-488G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112766 | |||||||
| chr12:113112812 | C | T | 1 | a0001c0001t0008g0035 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1182-534G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112812 | |||||||
| chr12:113112866 | C | T | 5 | a0002c0002t0002g0043 a0002c0002t0002g0044 a0002c0002t0002g0045 others(2): Show |
5 | HG02148.hp1 NA18960.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182-588G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112866 | |||||||
| chr12:113112939 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0212 |
2 | HG02080.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1182-661C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112939 | |||||||
| chr12:113112954 | A | AAAAT | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-680_1182-677d others(6): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112954 | |||||||
| chr12:113112954 | A | AAAATAAA others(1): Show |
156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1182-684_1182-677d others(10): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112954 | |||||||
| chr12:113112954 | A | AAAATAAA others(5): Show |
5 | a0001c0001t0001g0042 a0001c0001t0001g0107 a0001c0001t0001g0123 others(2): Show |
5 | HG04228.hp1 NA18946.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1182-688_1182-677d others(14): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112954 | |||||||
| chr12:113112954 | A | AAAATAAA others(9): Show |
1 | a0002c0002t0006g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1182-692_1182-677d others(18): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112954 | |||||||
| chr12:113112954 | A | AAAATAAA others(13): Show |
2 | a0002c0002t0001g0047 a0002c0019t0003g0033 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1182-696_1182-677d others(22): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112954 | |||||||
| chr12:113112954 | A | AAAATAAA others(17): Show |
1 | a0001c0001t0008g0035 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1182-677_1182-676i others(26): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113112954 | |||||||
| chr12:113113048 | G | A | 1 | a0002c0002t0006g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1182-770C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113048 | |||||||
| chr12:113113204 | C | T | 1 | a0004c0012t0001g0126 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1182-926G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113204 | |||||||
| chr12:113113316 | G | A | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-1038C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113316 | |||||||
| chr12:113113365 | C | T | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-1087G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113365 | |||||||
| chr12:113113428 | A | G | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1182-1150T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113428 | |||||||
| chr12:113113587 | A | G | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181+1213T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113587 | |||||||
| chr12:113113654 | T | C | 1 | a0002c0018t0004g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1181+1146A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113654 | |||||||
| chr12:113113720 | C | T | 8 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181+1080G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113720 | |||||||
| chr12:113113812 | C | A | 1 | a0001c0001t0008g0035 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1181+988G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113812 | |||||||
| chr12:113113883 | T | C | 5 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(2): Show |
5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181+917A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113883 | |||||||
| chr12:113113920 | A | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1181+880T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113920 | |||||||
| chr12:113113991 | A | G | 1 | a0002c0002t0001g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1181+809T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113113991 | |||||||
| chr12:113114189 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1181+611A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114189 | |||||||
| chr12:113114243 | C | T | 1 | a0012c0026t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1181+557G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114243 | |||||||
| chr12:113114298 | C | A | 2 | a0002c0002t0006g0034 a0002c0019t0003g0033 |
2 | HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1181+502G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114298 | |||||||
| chr12:113114335 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1181+465T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114335 | |||||||
| chr12:113114410 | G | A | 1 | a0002c0018t0004g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1181+390C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114410 | |||||||
| chr12:113114420 | G | A | 1 | a0008c0023t0005g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1181+380C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114420 | |||||||
| chr12:113114465 | C | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1181+335G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114465 | |||||||
| chr12:113114473 | CA | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1181+326delT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114473 | |||||||
| chr12:113114473 | CAA | C | 12 | a0001c0001t0001g0181 a0001c0001t0001g0206 a0002c0002t0002g0027 others(9): Show |
14 | HG01168.hp1 HG01168.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1181+325_1181+326d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114473 | |||||||
| chr12:113114491 | A | G | 1 | a0001c0007t0001g0082 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1181+309T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114491 | |||||||
| chr12:113114494 | A | G | 1 | a0002c0002t0006g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1181+306T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114494 | |||||||
| chr12:113114566 | C | T | 2 | a0002c0002t0006g0034 a0002c0019t0003g0033 |
2 | HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1181+234G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114566 | |||||||
| chr12:113114590 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1181+210G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114590 | |||||||
| chr12:113114652 | G | A | 7 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(4): Show |
9 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181+148C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114652 | |||||||
| chr12:113114746 | T | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0061 a0009c0015t0001g0151 |
3 | NA18946.hp1 NA18949.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1181+54A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 12/20 | chr12 | 113114746 | |||||||
| chr12:113115009 | G | T | 8 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(5): Show |
10 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1069-97C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 11/20 | chr12 | 113115009 | |||||||
| chr12:113115076 | G | A | 1 | a0002c0002t0001g0046 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1068+124C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 11/20 | chr12 | 113115076 | |||||||
| chr12:113115110 | G | A | 8 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(5): Show |
10 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1068+90C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 11/20 | chr12 | 113115110 | |||||||
| chr12:113115180 | G | C | 8 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(5): Show |
10 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1068+20C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 11/20 | chr12 | 113115180 | |||||||
| chr12:113115446 | C | T | 4 | a0001c0001t0001g0132 a0001c0001t0001g0144 a0001c0001t0001g0164 others(1): Show |
4 | HG01192.hp2 HG01255.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1004-182G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 10/20 | chr12 | 113115446 | |||||||
| chr12:113115460 | C | T | 2 | a0002c0008t0005g0039 a0002c0008t0005g0040 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1003+175G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 10/20 | chr12 | 113115460 | |||||||
| chr12:113115543 | C | T | 8 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(5): Show |
10 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1003+92G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 10/20 | chr12 | 113115543 | |||||||
| chr12:113115603 | C | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1003+32G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 10/20 | chr12 | 113115603 | |||||||
| chr12:113115615 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1003+20C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 10/20 | chr12 | 113115615 | |||||||
| chr12:113115624 | G | A | 2 | a0002c0008t0005g0039 a0002c0008t0005g0040 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1003+11C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 10/20 | chr12 | 113115624 | |||||||
| chr12:113115819 | C | T | 1 | a0002c0002t0001g0118 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.850-31G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 9/20 | chr12 | 113115819 | |||||||
| chr12:113115847 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.850-59G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 9/20 | chr12 | 113115847 | |||||||
| chr12:113115862 | G | A | 3 | a0002c0002t0003g0030 a0002c0002t0006g0034 a0002c0019t0003g0033 |
3 | HG02055.hp1 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.849+72C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 9/20 | chr12 | 113115862 | |||||||
| chr12:113115869 | AG | A | 5 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(2): Show |
5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+64delC | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 9/20 | chr12 | 113115869 | |||||||
| chr12:113116091 | C | T | 1 | a0012c0026t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.732-40G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116091 | |||||||
| chr12:113116095 | C | T | 18 | a0002c0002t0002g0004 a0002c0002t0002g0014 a0002c0002t0002g0043 others(15): Show |
24 | HG01123.hp1 HG02040.hp2 HG02148.hp1 others(21): Show |
intron_variant | MODIFIER | c.732-44G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116095 | |||||||
| chr12:113116107 | C | T | 1 | a0001c0001t0008g0035 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.732-56G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116107 | |||||||
| chr12:113116180 | AC | A | 7 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(4): Show |
9 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.732-130delG | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116180 | |||||||
| chr12:113116230 | C | T | 1 | a0002c0002t0002g0234 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.732-179G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116230 | |||||||
| chr12:113116319 | C | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0187 a0001c0001t0001g0213 |
3 | HG02630.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.732-268G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116319 | |||||||
| chr12:113116593 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0173 |
2 | HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.731+480C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116593 | |||||||
| chr12:113116624 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.731+449T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116624 | |||||||
| chr12:113116677 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.731+396C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116677 | |||||||
| chr12:113116803 | G | C | 1 | a0002c0003t0002g0066 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.731+270C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116803 | |||||||
| chr12:113116810 | G | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.731+263C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116810 | |||||||
| chr12:113116884 | G | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0098 others(9): Show |
15 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.731+189C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116884 | |||||||
| chr12:113116908 | T | C | 8 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(5): Show |
10 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.731+165A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113116908 | |||||||
| chr12:113117028 | C | T | 5 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(2): Show |
7 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.731+45G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 8/20 | chr12 | 113117028 | |||||||
| chr12:113117311 | TC | T | 5 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(2): Show |
7 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-151delG | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113117311 | |||||||
| chr12:113117495 | T | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.643-334A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113117495 | |||||||
| chr12:113117742 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.643-581T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113117742 | |||||||
| chr12:113117840 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.643-679G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113117840 | |||||||
| chr12:113117873 | G | GT | 6 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(3): Show |
6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-713dupA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113117873 | |||||||
| chr12:113118051 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.643-890G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113118051 | |||||||
| chr12:113118060 | T | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
5 | HG02258.hp2 HG02280.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-899A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113118060 | |||||||
| chr12:113118581 | G | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.642+547C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113118581 | |||||||
| chr12:113118608 | G | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0122 a0001c0001t0001g0133 others(8): Show |
16 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.642+520C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113118608 | |||||||
| chr12:113118894 | G | C | 1 | a0002c0002t0001g0046 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.642+234C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113118894 | |||||||
| chr12:113119000 | C | G | 5 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(2): Show |
5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.642+128G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 7/20 | chr12 | 113119000 | |||||||
| chr12:113119267 | C | T | 1 | a0002c0006t0004g0201 | 1 | HG00280.hp1 | splice_region_variant&intron_variant | LOW | c.511-8G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 6/20 | chr12 | 113119267 | |||||||
| chr12:113119268 | G | A | 9 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0118 others(6): Show |
11 | HG00642.hp1 HG00733.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.511-9C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 6/20 | chr12 | 113119268 | |||||||
| chr12:113119584 | C | T | 1 | a0002c0002t0001g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.429-141G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113119584 | |||||||
| chr12:113119596 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.429-153G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113119596 | |||||||
| chr12:113119772 | TG | T | 6 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(3): Show |
6 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.429-330delC | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113119772 | |||||||
| chr12:113119809 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429-366G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113119809 | |||||||
| chr12:113119870 | A | G | 2 | a0002c0003t0002g0071 a0002c0003t0002g0073 |
2 | NA18951.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.429-427T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113119870 | |||||||
| chr12:113120069 | A | G | 7 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(4): Show |
9 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.429-626T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120069 | |||||||
| chr12:113120172 | G | C | 5 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(2): Show |
7 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.429-729C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120172 | |||||||
| chr12:113120410 | C | T | 1 | a0012c0026t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.429-967G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120410 | |||||||
| chr12:113120452 | C | T | 2 | a0002c0008t0005g0039 a0002c0008t0005g0040 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.429-1009G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120452 | |||||||
| chr12:113120471 | C | T | 12 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(9): Show |
14 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.429-1028G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120471 | |||||||
| chr12:113120582 | C | G | 5 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(2): Show |
5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.428+927G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120582 | |||||||
| chr12:113120840 | T | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.428+669A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120840 | |||||||
| chr12:113120924 | G | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0141 a0001c0001t0001g0147 |
6 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.428+585C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113120924 | |||||||
| chr12:113121067 | T | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.428+442A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113121067 | |||||||
| chr12:113121084 | C | T | 1 | a0012c0026t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.428+425G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113121084 | |||||||
| chr12:113121281 | C | T | 1 | a0012c0026t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.428+228G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113121281 | |||||||
| chr12:113121322 | C | T | 1 | a0002c0019t0003g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.428+187G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 5/20 | chr12 | 113121322 | |||||||
| chr12:113121642 | A | G | 18 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(15): Show |
20 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(17): Show |
splice_region_variant&intron_variant | LOW | c.299-4T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113121642 | |||||||
| chr12:113121726 | ATT | A | 9 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(6): Show |
11 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-90_299-89delAA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113121726 | |||||||
| chr12:113121777 | A | T | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.299-139T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113121777 | |||||||
| chr12:113121800 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.299-162G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113121800 | |||||||
| chr12:113122065 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.299-427A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122065 | |||||||
| chr12:113122227 | C | T | 13 | a0002c0002t0002g0004 a0002c0002t0002g0014 a0002c0002t0002g0050 others(10): Show |
19 | HG01123.hp1 HG02040.hp2 HG02300.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-589G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122227 | |||||||
| chr12:113122234 | C | T | 1 | a0002c0002t0001g0046 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.299-596G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122234 | |||||||
| chr12:113122426 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0105 a0001c0001t0001g0124 others(1): Show |
7 | HG00642.hp2 HG00735.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-788G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122426 | |||||||
| chr12:113122506 | G | A | 1 | a0002c0002t0001g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.299-868C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122506 | |||||||
| chr12:113122544 | C | T | 13 | a0002c0002t0002g0004 a0002c0002t0002g0014 a0002c0002t0002g0050 others(10): Show |
19 | HG01123.hp1 HG02040.hp2 HG02300.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-906G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122544 | |||||||
| chr12:113122569 | C | T | 1 | a0005c0014t0001g0091 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.299-931G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122569 | |||||||
| chr12:113122574 | C | G | 2 | a0002c0003t0002g0071 a0002c0003t0002g0073 |
2 | NA18951.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.299-936G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122574 | |||||||
| chr12:113122601 | A | AGGCAGGA others(14): Show |
3 | a0002c0002t0003g0030 a0002c0002t0006g0034 a0002c0019t0003g0033 |
3 | HG02055.hp1 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.299-984_299-964dup others(21): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122601 | |||||||
| chr12:113122706 | A | T | 5 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(2): Show |
5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1068T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122706 | |||||||
| chr12:113122841 | T | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0098 others(10): Show |
16 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.299-1203A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122841 | |||||||
| chr12:113122850 | T | A | 1 | a0012c0026t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.299-1212A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122850 | |||||||
| chr12:113122966 | A | G | 3 | a0001c0001t0001g0159 a0001c0001t0001g0187 a0001c0001t0001g0213 |
3 | HG02630.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.299-1328T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113122966 | |||||||
| chr12:113123099 | C | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.299-1461G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123099 | |||||||
| chr12:113123144 | C | T | 1 | a0002c0018t0004g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.299-1506G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123144 | |||||||
| chr12:113123189 | C | T | 1 | a0004c0012t0001g0126 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.299-1551G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123189 | |||||||
| chr12:113123279 | A | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.299-1641T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123279 | |||||||
| chr12:113123466 | C | T | 3 | a0002c0002t0003g0030 a0002c0002t0006g0034 a0002c0019t0003g0033 |
3 | HG02055.hp1 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.299-1828G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123466 | |||||||
| chr12:113123513 | G | A | 5 | a0002c0006t0004g0089 a0002c0006t0004g0195 a0002c0006t0004g0201 others(2): Show |
5 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1875C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123513 | |||||||
| chr12:113123548 | CT | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.299-1911delA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123548 | |||||||
| chr12:113123568 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.299-1930C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123568 | |||||||
| chr12:113123708 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.299-2070G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123708 | |||||||
| chr12:113123826 | G | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(4): Show |
28 | HG00423.hp1 HG00558.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.299-2188C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123826 | |||||||
| chr12:113123923 | T | C | 3 | a0002c0002t0003g0030 a0002c0002t0006g0034 a0002c0019t0003g0033 |
3 | HG02055.hp1 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.299-2285A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123923 | |||||||
| chr12:113123926 | A | G | 14 | a0002c0002t0002g0004 a0002c0002t0002g0014 a0002c0002t0002g0050 others(11): Show |
20 | HG01123.hp1 HG02040.hp2 HG02300.hp1 others(17): Show |
intron_variant | MODIFIER | c.299-2288T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113123926 | |||||||
| chr12:113124090 | T | C | 22 | a0001c0001t0001g0042 a0001c0001t0001g0061 a0002c0002t0002g0004 others(19): Show |
28 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.299-2452A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124090 | |||||||
| chr12:113124133 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.299-2495C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124133 | |||||||
| chr12:113124174 | T | C | 1 | a0002c0003t0002g0076 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.299-2536A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124174 | |||||||
| chr12:113124209 | C | A | 14 | a0002c0002t0002g0004 a0002c0002t0002g0014 a0002c0002t0002g0050 others(11): Show |
20 | HG01123.hp1 HG02040.hp2 HG02300.hp1 others(17): Show |
intron_variant | MODIFIER | c.299-2571G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124209 | |||||||
| chr12:113124217 | C | CA | 9 | a0001c0001t0001g0204 a0001c0001t0001g0229 a0001c0001t0001g0230 others(6): Show |
10 | HG01891.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-2580dupT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124217 | |||||||
| chr12:113124217 | CA | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
159 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.299-2580delT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124217 | |||||||
| chr12:113124217 | CAA | C | 34 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(31): Show |
47 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.299-2581_299-2580d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124217 | |||||||
| chr12:113124239 | A | AAT | 21 | a0001c0001t0001g0042 a0001c0001t0001g0061 a0001c0001t0001g0123 others(18): Show |
27 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.299-2602_299-2601i others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124239 | |||||||
| chr12:113124239 | A | AT | 10 | a0001c0001t0003g0031 a0001c0001t0008g0035 a0002c0002t0001g0021 others(7): Show |
12 | HG00642.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-2602_299-2601i others(3): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124239 | |||||||
| chr12:113124239 | A | T | 1 | a0002c0002t0001g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.299-2601T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124239 | |||||||
| chr12:113124535 | C | A | 1 | a0001c0001t0003g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.299-2897G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124535 | |||||||
| chr12:113124670 | A | G | 22 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0025 others(19): Show |
29 | HG01081.hp2 HG01099.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.299-3032T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124670 | |||||||
| chr12:113124726 | T | C | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0003g0031 |
3 | HG01891.hp2 HG02559.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.298+3086A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124726 | |||||||
| chr12:113124745 | C | T | 2 | a0002c0002t0003g0030 a0002c0002t0006g0034 |
2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.298+3067G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124745 | |||||||
| chr12:113124882 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.298+2930T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124882 | |||||||
| chr12:113124895 | T | G | 1 | a0008c0023t0005g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.298+2917A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124895 | |||||||
| chr12:113124916 | T | C | 2 | a0002c0008t0005g0039 a0002c0008t0005g0040 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.298+2896A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113124916 | |||||||
| chr12:113125012 | G | A | 3 | a0002c0002t0002g0050 a0002c0002t0002g0056 a0002c0003t0002g0078 |
3 | NA18945.hp1 NA18975.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.298+2800C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125012 | |||||||
| chr12:113125097 | T | TA | 34 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0087 others(31): Show |
42 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(39): Show |
intron_variant | MODIFIER | c.298+2714dupT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125097 | |||||||
| chr12:113125097 | TA | T | 23 | a0001c0001t0001g0098 a0001c0001t0001g0123 a0001c0001t0001g0124 others(20): Show |
25 | HG00558.hp2 HG01071.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.298+2714delT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125097 | |||||||
| chr12:113125122 | CAT | C | 3 | a0001c0001t0001g0087 a0001c0001t0001g0114 a0001c0001t0001g0186 |
3 | NA18948.hp1 NA18954.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.298+2688_298+2689d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125122 | |||||||
| chr12:113125167 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.298+2645C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125167 | |||||||
| chr12:113125300 | C | T | 68 | a0001c0001t0001g0017 a0001c0001t0001g0051 a0001c0001t0001g0057 others(65): Show |
83 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.298+2512G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125300 | |||||||
| chr12:113125316 | G | A | 33 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0008g0035 others(30): Show |
42 | HG00280.hp2 HG02040.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.298+2496C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125316 | |||||||
| chr12:113125708 | G | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG02056.hp2 NA18949.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.298+2104C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125708 | |||||||
| chr12:113125762 | G | T | 26 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0008g0035 others(23): Show |
34 | HG02040.hp2 HG02055.hp1 HG02080.hp2 others(31): Show |
intron_variant | MODIFIER | c.298+2050C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125762 | |||||||
| chr12:113125947 | A | G | 1 | a0002c0002t0001g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.298+1865T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113125947 | |||||||
| chr12:113126087 | C | A | 1 | a0002c0002t0002g0043 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.298+1725G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126087 | |||||||
| chr12:113126111 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.298+1701G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126111 | |||||||
| chr12:113126142 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.298+1670C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126142 | |||||||
| chr12:113126182 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0135 a0001c0001t0001g0152 others(2): Show |
6 | HG01943.hp2 HG02572.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+1630C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126182 | |||||||
| chr12:113126280 | G | A | 2 | a0002c0002t0003g0037 a0002c0019t0003g0033 |
2 | HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.298+1532C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126280 | |||||||
| chr12:113126295 | A | T | 1 | a0002c0002t0006g0032 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.298+1517T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126295 | |||||||
| chr12:113126488 | G | A | 2 | a0002c0003t0002g0110 a0002c0003t0002g0228 |
2 | NA18956.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.298+1324C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126488 | |||||||
| chr12:113126688 | T | A | 1 | a0003c0010t0007g0029 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.298+1124A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | |||||||
| chr12:113126688 | T | TCA | 27 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(24): Show |
44 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.298+1122_298+1123d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | |||||||
| chr12:113126688 | T | TCACA | 10 | a0001c0001t0001g0147 a0001c0001t0001g0187 a0001c0001t0001g0188 others(7): Show |
10 | HG00140.hp2 HG01891.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+1120_298+1123d others(6): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | |||||||
| chr12:113126688 | T | TCACACA | 15 | a0001c0007t0001g0070 a0001c0007t0001g0072 a0002c0003t0001g0074 others(12): Show |
18 | HG00438.hp2 HG02155.hp1 NA18945.hp2 others(15): Show |
intron_variant | MODIFIER | c.298+1118_298+1123d others(8): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | |||||||
| chr12:113126688 | T | TCACACAC others(1): Show |
4 | a0002c0003t0002g0079 a0002c0003t0002g0080 a0002c0003t0002g0083 others(1): Show |
4 | HG02622.hp2 NA18954.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+1116_298+1123d others(10): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | |||||||
| chr12:113126688 | T | TCACACAC others(7): Show |
1 | a0001c0007t0001g0082 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.298+1110_298+1123d others(16): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | |||||||
| chr12:113126688 | TCA | T | 11 | a0001c0001t0001g0023 a0001c0001t0001g0134 a0001c0001t0001g0135 others(8): Show |
12 | HG01943.hp2 HG02572.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.298+1122_298+1123d others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | |||||||
| chr12:113126688 | TCACA | T | 14 | a0001c0001t0001g0065 a0001c0001t0001g0107 a0001c0001t0001g0133 others(11): Show |
16 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.298+1120_298+1123d others(6): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | |||||||
| chr12:113126688 | TCACACA | T | 16 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0002c0002t0002g0004 others(13): Show |
22 | HG02040.hp2 HG02080.hp2 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.298+1118_298+1123d others(8): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126688 | |||||||
| chr12:113126690 | A | T | 5 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0004t0001g0015 others(2): Show |
6 | HG02717.hp2 HG03195.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+1122T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126690 | |||||||
| chr12:113126692 | A | T | 3 | a0001c0004t0001g0015 a0001c0004t0001g0064 a0012c0026t0002g0048 |
4 | HG02717.hp2 HG03195.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+1120T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126692 | |||||||
| chr12:113126694 | A | T | 8 | a0001c0001t0001g0065 a0002c0002t0002g0027 a0002c0002t0002g0028 others(5): Show |
10 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+1118T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126694 | |||||||
| chr12:113126696 | A | T | 12 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0002c0002t0002g0004 others(9): Show |
18 | HG02040.hp2 HG02080.hp2 HG02300.hp1 others(15): Show |
intron_variant | MODIFIER | c.298+1116T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126696 | |||||||
| chr12:113126698 | A | T | 2 | a0001c0001t0001g0051 a0002c0018t0004g0041 |
2 | HG02080.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.298+1114T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126698 | |||||||
| chr12:113126765 | A | C | 1 | a0002c0018t0004g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.298+1047T>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126765 | |||||||
| chr12:113126769 | C | T | 4 | a0002c0002t0002g0028 a0002c0002t0002g0232 a0002c0002t0002g0233 others(1): Show |
5 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+1043G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126769 | |||||||
| chr12:113126815 | T | C | 65 | a0001c0001t0001g0017 a0001c0001t0001g0051 a0001c0001t0001g0057 others(62): Show |
78 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.298+997A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126815 | |||||||
| chr12:113126928 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.298+884A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126928 | |||||||
| chr12:113126944 | T | C | 3 | a0001c0004t0001g0015 a0001c0004t0001g0064 a0012c0026t0002g0048 |
4 | HG02717.hp2 HG03195.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.298+868A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126944 | |||||||
| chr12:113126950 | A | ATTATTAT others(25): Show |
27 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0008g0035 others(24): Show |
35 | HG02040.hp2 HG02055.hp1 HG02080.hp2 others(32): Show |
intron_variant | MODIFIER | c.298+830_298+861dup others(32): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113126950 | |||||||
| chr12:113127067 | T | TAAATTAT others(38): Show |
1 | a0001c0001t0001g0132 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.298+744_298+745ins others(45): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127067 | |||||||
| chr12:113127069 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.298+743T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127069 | |||||||
| chr12:113127070 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.298+742C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127070 | |||||||
| chr12:113127119 | G | C | 25 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0002c0002t0001g0021 others(22): Show |
35 | HG02040.hp2 HG02055.hp2 HG02080.hp2 others(32): Show |
intron_variant | MODIFIER | c.298+693C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127119 | |||||||
| chr12:113127267 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG01099.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.298+545T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127267 | |||||||
| chr12:113127430 | G | T | 31 | a0001c0001t0001g0017 a0001c0001t0001g0116 a0001c0001t0001g0117 others(28): Show |
35 | HG00438.hp2 HG00642.hp1 HG02071.hp2 others(32): Show |
intron_variant | MODIFIER | c.298+382C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127430 | |||||||
| chr12:113127523 | A | C | 1 | a0002c0002t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.298+289T>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127523 | |||||||
| chr12:113127527 | G | A | 1 | a0002c0002t0001g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.298+285C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127527 | |||||||
| chr12:113127543 | C | G | 32 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0008g0035 others(29): Show |
42 | HG02040.hp2 HG02055.hp1 HG02055.hp2 others(39): Show |
intron_variant | MODIFIER | c.298+269G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127543 | |||||||
| chr12:113127578 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0016 others(17): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.298+234C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127578 | |||||||
| chr12:113127606 | C | T | 1 | a0006c0009t0002g0038 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.298+206G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127606 | |||||||
| chr12:113127612 | C | T | 12 | a0001c0001t0008g0035 a0001c0004t0001g0015 a0001c0004t0001g0064 others(9): Show |
13 | HG00280.hp2 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.298+200G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127612 | |||||||
| chr12:113127735 | G | A | 8 | a0001c0001t0008g0035 a0002c0002t0003g0030 a0002c0002t0003g0037 others(5): Show |
8 | HG02055.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+77C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 4/20 | chr12 | 113127735 | |||||||
| chr12:113127918 | T | G | 1 | a0002c0003t0002g0067 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.237-45A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/20 | chr12 | 113127918 | |||||||
| chr12:113127919 | G | C | 1 | a0002c0003t0002g0067 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.237-46C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/20 | chr12 | 113127919 | |||||||
| chr12:113127923 | C | T | 1 | a0008c0023t0005g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.237-50G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/20 | chr12 | 113127923 | |||||||
| chr12:113127982 | G | C | 1 | a0002c0002t0001g0231 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.236+83C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/20 | chr12 | 113127982 | |||||||
| chr12:113127997 | C | T | 13 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0002c0002t0002g0004 others(10): Show |
19 | HG02040.hp2 HG02080.hp2 HG02300.hp1 others(16): Show |
intron_variant | MODIFIER | c.236+68G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 3/20 | chr12 | 113127997 | |||||||
| chr12:113128245 | G | GAC | 30 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(27): Show |
52 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.123-69_123-68dupGT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | |||||||
| chr12:113128245 | G | GACAC | 3 | a0001c0001t0001g0212 a0002c0003t0002g0068 a0002c0006t0004g0201 |
3 | HG00280.hp1 NA18747.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.123-71_123-68dupGT others(2): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | |||||||
| chr12:113128245 | G | GACACAC | 17 | a0001c0007t0001g0070 a0001c0007t0001g0072 a0002c0003t0001g0074 others(14): Show |
20 | HG00438.hp2 HG02071.hp2 NA18945.hp2 others(17): Show |
intron_variant | MODIFIER | c.123-73_123-68dupGT others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | |||||||
| chr12:113128245 | G | GACACACA others(1): Show |
3 | a0002c0003t0002g0081 a0002c0003t0002g0084 a0006c0009t0002g0038 |
3 | HG02155.hp1 HG02622.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.123-75_123-68dupGT others(6): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | |||||||
| chr12:113128245 | G | GACACACA others(3): Show |
1 | a0001c0007t0001g0082 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.123-77_123-68dupGT others(8): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | |||||||
| chr12:113128245 | G | GACACACA others(9): Show |
1 | a0001c0001t0003g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123-83_123-68dupGT others(14): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | |||||||
| chr12:113128245 | GAC | G | 46 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0018 others(43): Show |
55 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.123-69_123-68delGT | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | |||||||
| chr12:113128245 | GACAC | G | 11 | a0001c0001t0001g0017 a0001c0001t0001g0116 a0001c0001t0001g0117 others(8): Show |
12 | HG00642.hp1 HG01358.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.123-71_123-68delGT others(2): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | |||||||
| chr12:113128245 | GACACAC | G | 3 | a0002c0008t0005g0039 a0002c0008t0005g0040 a0008c0023t0005g0111 |
3 | HG02572.hp2 HG03471.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.123-73_123-68delGT others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | |||||||
| chr12:113128245 | GACACACA others(1): Show |
G | 24 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0008g0035 others(21): Show |
32 | HG00280.hp2 HG02040.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.123-75_123-68delGT others(6): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | |||||||
| chr12:113128245 | GACACACA others(5): Show |
G | 1 | a0012c0026t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123-79_123-68delGT others(10): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128245 | |||||||
| chr12:113128282 | G | C | 1 | a0002c0003t0002g0083 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.123-104C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128282 | |||||||
| chr12:113128490 | A | AAC | 10 | a0001c0001t0001g0092 a0001c0001t0001g0130 a0001c0001t0001g0131 others(7): Show |
10 | HG00741.hp2 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.123-314_123-313dup others(2): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128490 | |||||||
| chr12:113128512 | C | CACAG | 20 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0002c0002t0002g0004 others(17): Show |
28 | HG02040.hp2 HG02080.hp2 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.123-335_123-334ins others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128512 | |||||||
| chr12:113128512 | C | G | 3 | a0002c0002t0006g0032 a0002c0018t0004g0041 a0003c0010t0007g0029 |
3 | HG00280.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.123-334G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128512 | |||||||
| chr12:113128630 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.123-452G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128630 | |||||||
| chr12:113128676 | C | T | 1 | a0003c0010t0007g0029 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.123-498G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128676 | |||||||
| chr12:113128712 | C | T | 2 | a0001c0001t0001g0095 a0002c0002t0001g0231 |
2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.123-534G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128712 | |||||||
| chr12:113128839 | A | G | 1 | a0013c0024t0003g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.123-661T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128839 | |||||||
| chr12:113128972 | G | GAC | 39 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0104 others(36): Show |
45 | HG01168.hp1 HG01346.hp2 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.123-796_123-795dup others(2): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128972 | |||||||
| chr12:113128972 | G | GACAC | 18 | a0001c0001t0001g0017 a0001c0001t0001g0117 a0001c0001t0001g0213 others(15): Show |
20 | HG00642.hp1 HG02055.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.123-798_123-795dup others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128972 | |||||||
| chr12:113128972 | G | GACACAC | 24 | a0001c0001t0001g0087 a0001c0007t0001g0070 a0001c0007t0001g0072 others(21): Show |
28 | HG00438.hp2 HG02040.hp2 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.123-800_123-795dup others(6): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128972 | |||||||
| chr12:113128972 | GAC | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
6 | HG02602.hp2 HG02647.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-796_123-795del others(2): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128972 | |||||||
| chr12:113128972 | GACAC | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0005t0001g0221 |
3 | HG01099.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.123-798_123-795del others(4): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113128972 | |||||||
| chr12:113129067 | C | G | 1 | a0004c0012t0001g0126 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.123-889G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129067 | |||||||
| chr12:113129124 | C | A | 13 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0002c0002t0002g0004 others(10): Show |
19 | HG02040.hp2 HG02080.hp2 HG02300.hp1 others(16): Show |
intron_variant | MODIFIER | c.123-946G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129124 | |||||||
| chr12:113129232 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0125 |
3 | HG01099.hp2 HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.123-1054G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129232 | |||||||
| chr12:113129361 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123-1183G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129361 | |||||||
| chr12:113129557 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.122+1328C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129557 | |||||||
| chr12:113129713 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.122+1172G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129713 | |||||||
| chr12:113129721 | C | T | 28 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0008g0035 others(25): Show |
37 | HG02040.hp2 HG02055.hp1 HG02080.hp2 others(34): Show |
intron_variant | MODIFIER | c.122+1164G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129721 | |||||||
| chr12:113129722 | G | A | 1 | a0013c0024t0003g0036 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.122+1163C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129722 | |||||||
| chr12:113129722 | G | GCACA | 3 | a0002c0008t0005g0039 a0002c0008t0005g0040 a0002c0018t0004g0041 |
3 | HG02572.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.122+1159_122+1162d others(6): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129722 | |||||||
| chr12:113129738 | A | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.122+1147T>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113129738 | |||||||
| chr12:113130044 | G | A | 1 | a0002c0018t0004g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.122+841C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130044 | |||||||
| chr12:113130049 | G | T | 1 | a0008c0023t0005g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.122+836C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130049 | |||||||
| chr12:113130094 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.122+791T>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130094 | |||||||
| chr12:113130253 | C | T | 1 | a0001c0022t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.122+632G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130253 | |||||||
| chr12:113130273 | T | G | 1 | a0001c0001t0003g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.122+612A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130273 | |||||||
| chr12:113130421 | C | A | 6 | a0001c0001t0008g0035 a0002c0002t0003g0030 a0002c0002t0003g0037 others(3): Show |
6 | HG02055.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+464G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130421 | |||||||
| chr12:113130450 | T | G | 2 | a0001c0001t0001g0121 a0003c0010t0007g0029 |
2 | HG00280.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.122+435A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130450 | |||||||
| chr12:113130457 | G | A | 2 | a0001c0001t0003g0031 a0002c0002t0006g0032 |
2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.122+428C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130457 | |||||||
| chr12:113130514 | C | G | 57 | a0001c0001t0001g0017 a0001c0001t0001g0051 a0001c0001t0001g0057 others(54): Show |
70 | HG00438.hp2 HG00642.hp1 HG02040.hp2 others(67): Show |
intron_variant | MODIFIER | c.122+371G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130514 | |||||||
| chr12:113130529 | A | G | 67 | a0001c0001t0001g0017 a0001c0001t0001g0051 a0001c0001t0001g0057 others(64): Show |
80 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.122+356T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130529 | |||||||
| chr12:113130536 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0003g0031 a0003c0010t0007g0029 |
3 | HG00280.hp2 HG01361.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.122+349G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130536 | |||||||
| chr12:113130601 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.122+284C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130601 | |||||||
| chr12:113130612 | G | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0116 a0001c0001t0001g0117 others(4): Show |
8 | HG00642.hp1 HG02148.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+273C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130612 | |||||||
| chr12:113130690 | G | A | 1 | a0002c0002t0002g0219 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.122+195C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130690 | |||||||
| chr12:113130772 | C | A | 15 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0002g0060 others(12): Show |
21 | HG02040.hp2 HG02080.hp2 HG02300.hp1 others(18): Show |
intron_variant | MODIFIER | c.122+113G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 2/20 | chr12 | 113130772 | |||||||
| chr12:113130943 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG03942.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.66-2A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113130943 | |||||||
| chr12:113130992 | A | G | 70 | a0001c0001t0001g0017 a0001c0001t0001g0051 a0001c0001t0001g0057 others(67): Show |
83 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.66-51T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113130992 | |||||||
| chr12:113131056 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG02056.hp2 NA18949.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.66-115G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131056 | |||||||
| chr12:113131100 | G | A | 1 | a0001c0005t0001g0221 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.66-159C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131100 | |||||||
| chr12:113131168 | A | G | 3 | a0002c0008t0005g0039 a0002c0008t0005g0040 a0002c0018t0004g0041 |
3 | HG02572.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.66-227T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131168 | |||||||
| chr12:113131247 | T | G | 5 | a0001c0001t0001g0222 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.66-306A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131247 | |||||||
| chr12:113131248 | G | T | 1 | a0001c0001t0001g0017 | 2 | HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.66-307C>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131248 | |||||||
| chr12:113131250 | G | C | 1 | a0001c0001t0001g0087 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.66-309C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131250 | |||||||
| chr12:113131383 | G | A | 2 | a0002c0002t0001g0046 a0002c0002t0001g0047 |
2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.66-442C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131383 | |||||||
| chr12:113131434 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.66-493G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131434 | |||||||
| chr12:113131643 | T | C | 1 | a0001c0017t0001g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.66-702A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131643 | |||||||
| chr12:113131857 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.66-916G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131857 | |||||||
| chr12:113131932 | C | T | 12 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0096 others(9): Show |
13 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.66-991G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131932 | |||||||
| chr12:113131964 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.66-1023A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131964 | |||||||
| chr12:113131968 | C | CT | 10 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(7): Show |
11 | HG00642.hp1 HG00673.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.66-1028dupA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131968 | |||||||
| chr12:113131968 | CT | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0105 others(17): Show |
21 | HG00323.hp2 HG00408.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.66-1028delA | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131968 | |||||||
| chr12:113131968 | CTT | C | 52 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0061 others(49): Show |
59 | HG00408.hp2 HG00438.hp2 HG02040.hp1 others(56): Show |
intron_variant | MODIFIER | c.66-1029_66-1028del others(2): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131968 | |||||||
| chr12:113131983 | T | G | 1 | a0002c0003t0002g0228 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.66-1042A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113131983 | |||||||
| chr12:113132074 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.66-1133G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132074 | |||||||
| chr12:113132239 | T | C | 58 | a0001c0001t0001g0051 a0001c0001t0001g0057 a0001c0001t0001g0061 others(55): Show |
70 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.66-1298A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132239 | |||||||
| chr12:113132269 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.66-1328C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132269 | |||||||
| chr12:113132456 | C | A | 1 | a0002c0002t0002g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.66-1515G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132456 | |||||||
| chr12:113132456 | C | T | 24 | a0001c0001t0001g0065 a0001c0001t0001g0085 a0001c0001t0001g0087 others(21): Show |
27 | HG00408.hp2 HG00438.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.66-1515G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132456 | |||||||
| chr12:113132457 | G | C | 1 | a0002c0002t0002g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.66-1516C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132457 | |||||||
| chr12:113132524 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.66-1583G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132524 | |||||||
| chr12:113132792 | C | A | 1 | a0002c0002t0001g0231 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.66-1851G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132792 | |||||||
| chr12:113132879 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.66-1938G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132879 | |||||||
| chr12:113132945 | C | T | 2 | a0001c0001t0001g0006 a0005c0014t0001g0091 |
6 | HG02132.hp2 NA18956.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.66-2004G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113132945 | |||||||
| chr12:113133063 | G | A | 2 | a0001c0004t0001g0015 a0001c0004t0001g0064 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.66-2122C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133063 | |||||||
| chr12:113133111 | C | T | 1 | a0003c0010t0007g0029 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.66-2170G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133111 | |||||||
| chr12:113133379 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.65+2019G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133379 | |||||||
| chr12:113133532 | T | C | 26 | a0001c0001t0001g0065 a0001c0001t0001g0085 a0001c0001t0001g0087 others(23): Show |
29 | HG00408.hp2 HG00438.hp2 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.65+1866A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133532 | |||||||
| chr12:113133564 | T | C | 1 | a0002c0002t0002g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.65+1834A>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133564 | |||||||
| chr12:113133565 | C | T | 1 | a0002c0002t0002g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.65+1833G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133565 | |||||||
| chr12:113133568 | G | C | 1 | a0002c0002t0002g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.65+1830C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133568 | |||||||
| chr12:113133953 | C | G | 1 | a0002c0006t0004g0089 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.65+1445G>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113133953 | |||||||
| chr12:113134096 | AGGCCGTC others(10): Show |
A | 6 | a0001c0001t0008g0035 a0002c0002t0003g0030 a0002c0002t0003g0037 others(3): Show |
6 | HG02055.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.65+1285_65+1301del others(17): Show |
RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134096 | |||||||
| chr12:113134241 | T | G | 1 | a0002c0002t0002g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.65+1157A>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134241 | |||||||
| chr12:113134250 | T | A | 1 | a0002c0002t0002g0088 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.65+1148A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134250 | |||||||
| chr12:113134361 | A | G | 69 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0057 others(66): Show |
81 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.65+1037T>C | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134361 | |||||||
| chr12:113134493 | G | A | 5 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0232 others(2): Show |
7 | HG02280.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.65+905C>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134493 | |||||||
| chr12:113134772 | G | C | 1 | a0001c0001t0001g0235 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.65+626C>G | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134772 | |||||||
| chr12:113134846 | C | T | 1 | a0002c0002t0003g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.65+552G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134846 | |||||||
| chr12:113134929 | A | T | 1 | a0002c0002t0003g0037 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65+469T>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134929 | |||||||
| chr12:113134930 | T | A | 1 | a0002c0002t0003g0037 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65+468A>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113134930 | |||||||
| chr12:113135059 | C | A | 1 | a0002c0002t0003g0037 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65+339G>T | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113135059 | |||||||
| chr12:113135173 | C | T | 8 | a0001c0001t0003g0031 a0001c0001t0008g0035 a0002c0002t0003g0030 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.65+225G>A | RASAL1 | ENSG00000111344.12 | transcript | ENST00000548055.2 | protein_coding | 1/20 | chr12 | 113135173 |